Medical Device Manufacturer · GB , Aston Clinton

Zethon, Ltd.

2 submissions · 2 cleared · Since 2021
2
Total
2
Cleared
0
Denied

Zethon, Ltd. — FDA 510(k) Submissions

Zethon, Ltd. has submitted 2 FDA 510(k) premarket notifications since 2021, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Motor, Drill, Electric, Drill, Surgical, Ent (electric Or Pneumatic) Including Handpiece . Use the specialty filter in the sidebar to narrow results.

2 devices
1–2 of 2
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All2 Ear, Nose, Throat 1 Neurology 1